Paraoxonase gene polymorphisms and plasma oxidized low-density lipoprotein level as possible risk factors for exudative age-related macular degeneration

PURPOSE: Paraoxonase (E.C.3.1.1.2) is a polymorphic protein shown to prevent low-density lipoprotein oxidation. Our purpose is to evaluate the hypothesis that paraoxonase gene polymorphisms and plasma oxidized low-density lipoprotein level play a role in the occurrence of exudative age-related macul...

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Veröffentlicht in:American journal of ophthalmology 2001-08, Vol.132 (2), p.191-195
Hauptverfasser: Ikeda, Tsunehiko, Obayashi, Hiroshi, Hasegawa, Gouji, Nakamura, Naoto, Yoshikawa, Toshikazu, Imamura, Yutaka, Koizumi, Kan, Kinoshita, Shigeru
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Sprache:eng
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Zusammenfassung:PURPOSE: Paraoxonase (E.C.3.1.1.2) is a polymorphic protein shown to prevent low-density lipoprotein oxidation. Our purpose is to evaluate the hypothesis that paraoxonase gene polymorphisms and plasma oxidized low-density lipoprotein level play a role in the occurrence of exudative age-related macular degeneration. METHODS: We analyzed paraoxonase genotypes (A/B, Gln-Arg192 and L/M, Leu-Met54) and plasma oxidized low-density lipoprotein levels in 72 unrelated Japanese patients with exudative age-related macular degeneration and compared the results with those of 140 age-matched and sex-matched control subjects. RESULTS: The distribution of paraoxonase 192 and paraoxonase 54 polymorphisms was significantly different between the patients with age-related macular degeneration and control subjects (chi-square = 6.226, P = .0445, and chi-square = 6.863, P = .0323, respectively). The high frequency of the BB genotype at position 192 was observed in the exudative age-related macular degeneration group compared with control subjects (52.8% vs 35.0%, respectively; P = .0127). The high frequency of the LL genotype at position 54 was observed in the patients more than the controls (91.7% vs 77.1%, respectively; P = .0090). The mean (± SE) oxidized low-density lipoprotein levels in the patients was significantly higher than in the controls (19.1 ± 1.0 vs 16.2 ± 0.6 U/ml, P < .01). CONCLUSION: These results indicate that the paraoxonase gene polymorphisms may represent a possible genetic risk factor for age-related macular degeneration and that increased plasma oxidized low-density lipoprotein may be involved in the pathogenesis of age-related macular degeneration.
ISSN:0002-9394
1879-1891
DOI:10.1016/S0002-9394(01)00975-8